System and method for catheter-based septal defect repair

ABSTRACT

The contents include occlusion and/or repair of congenital heart defects including methods, apparatuses, and systems utilizing catheter delivery in order to repair congenital heart defects. In particular, a method of repair includes suturing a septal tissue proximate defect in order to repair the defect with a device introduced through a bodily lumen of a patient. A repair device can include an expansion assembly, a suture delivering portion, and a suture receiving portion.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. Ser. No. 10/976,395, filedOct. 29, 2004, now U.S. Pat. No. 7,722,629, issued May 25, 2010, andentitled “System and Method for Catheter-Based Septal Defect Repair”;the entire teachings of which are incorporated herein by reference.

FIELD OF THE DISCLOSURE

The present disclosure relates generally to occlusion and/or repair ofdefects of the heart. More specifically, the present disclosure relatesto methods, apparatuses and systems utilizing catheter delivery througha bodily lumen of a patient in order to repair congenital heart defects.

BACKGROUND

Congenital heart disease occurs in approximately six to ten childrenborn out of one thousand. In general terms, congenital heart defects areabnormalities in heart structure formation arising during fetaldevelopment. While symptoms of such defects may become apparentfollowing childbirth or early childhood, the presence of such defects,and symptoms arising therefrom, may not be recognized until well laterinto adulthood.

Congenital heart defects include, for example, Atrial Septal Defects(ASDs), Ventricular Septal Defects (VSDs), and Patent Ductus Arteriosis(PDA). Generally speaking, defects in the septum such as ASDs and VSDsare some of the most commonly occurring congenital heart defects. Forreference, the septum is composed of muscular tissue and acts to dividethe heart into left and right sides. More specifically, the septumincludes an atrial septum and a ventricular septum. As the nameindicates, ASDs include improper formation of the atrial septum, thewall separating the right atrium and the left atrium. VSDs are generallya hole or other defect in the ventricular septum, the wall separatingthe right ventricle and the left ventricle. The presence of suchcongenital heart defects can result in relatively mild symptoms such asdecreased energy, shortness of breath, or increased rate of fatigue.However, congenital heart defects can also lead to more serious problemsincluding heart failure, irreversible pulmonary vascular disease, orparadoxic embolization.

One type of ASD is a Patent Foramen Ovale (“PFO”). During fetaldevelopment a passageway for blood exists between a septum primum and aseptum secundum, which later combine to form the atrial septum. Thispassage, or opening, is used during fetal development to facilitateblood flow between the two atria in a growing fetus. In non-defectivehearts, the opening closes following childbirth due to increasedpressure on the left side of the heart. However, in instances where theatrial septum is defective, the passageway remains active afterchildbirth. This residual opening is a Patent Foramen Ovale. PFOs can besaid to act like selective valves in many cases. In operation, the“valve” might only open under certain pressure conditions. For instance,pressure exerted on the heart when a person is sneezing or otherwisestraining himself or herself can cause reverse blood flow through a PFO.

In the past, congenital heart defects have largely been treated throughopen-chest surgery or other invasive procedures requiring access throughthe chest or torso. Closure, or alternatively occlusion, of somecongenital defects has also been accomplished utilizing percutaneoustechniques. In particular, a transcatheter approach has been utilized todeliver occlusion devices for ASDs, PDAs, PFOs, and VSDs, for example.Generally, these occlusion devices are delivered to a septal defect andthen expanded within the defect in order to both occlude the defect, andanchor the occlusion device in a desired position.

However, the occlusion device technologies mentioned above arepotentially hampered by inherent shortcomings. For example, occlusiondevices are often limited to use with centrally located defects havingboth well-defined margins and limited sizes. Furthermore, implantationfailures including device migration, embolization, and residual shuntsoccur at undesirable levels. Indeed, repair of such failures can requireemergency open chest surgery. Additionally, holes at the bottom of theatrial septum and large holes in the middle of the atrial septum can beproblematic to occlusion device use, and may still require open chestsurgery in order to either suture a defect closed, or suture a patch tothe defect.

While catheter-based methods can include the shortcomings mentionedabove, open chest surgery is still less desirable than less invasivecatheter-based methods. In particular, during open chest surgery theheart is normally put under cardioplegic arrest with circulationmaintained by cardiopulmonary bypass. The invasiveness of suchprocedures, as well as stoppage of the heart, drastically increases therisks of death and prolonged recovery. As such, a need exists formethods and associated devices capable of repairing congenital defectsvia less invasive means, including repairing those defects not amenableto the use of occlusion devices. More specifically, a need exists for amethod and apparatus capable of allowing a surgeon to suture a septaldefect, or suture a patch to a septal defect, utilizing a catheterdelivery method.

SUMMARY

One aspect of the present disclosure relates to a method of repairing aseptal defect in a septum defined by septal tissue. In particular themethod includes introducing a guiding catheter into a bodily lumen of apatient and delivering a repair device proximate the septal defect viathe guiding catheter. The repair device can include a suture deliveringportion maintaining a suture and a suture receiving portion. Opposingsides of the septum are pressed together with the repair device.Further, the suture is positioned at a first location proximate theseptal defect with the repair device and driven through the tissue atthe first location with the repair device. The suture is positioned at asecond location proximate the septal defect and driven through thetissue at the second location with the repair device. Additionally, thesuture is captured with the repair device and tied to repair the defect.

Another aspect of the present disclosure includes positioning a firstend of the suture at the first location proximate the septal defect anddriving the first end of the suture from a first side of the septum to asecond side of the septum with the suture delivering portion of therepair device. The suture is positioned at the second location proximatethe septal defect by positioning a second end of the suture at thesecond location proximate the septal defect. The second end of thesuture is driven from the first side of the septum to the second side ofthe septum with the suture delivering portion. The first and second endsof the suture are captured with the suture receiving portion at thesecond side of the septum.

Yet another aspect of the present disclosure includes positioning thesuture at the first location with the repair device by positioning afirst end of the suture at the first location proximate the septaldefect. The suture is driven through the tissue at the first location bydriving the first end of the suture from a first side of the septum to asecond side of the septum with the suture delivering portion. The firstend of the suture is positioned at the second location proximate theseptal defect and driven from the second side of the septum to the firstside of the septum with the suture delivering portion. The first end ofthe suture is captured with the suture receiving portion at the firstside of the septum and the suture is tied.

Another aspect of the present disclosure relates to a septal defectrepair system for repairing a septal defect in a septum defined byseptal tissue. In particular, the system comprises a guide catheterdisposed within a bodily lumen of a patient and a repair device disposedwithin the guide catheter. The repair device includes an expansionassembly configured to press opposing sides of the septum together and asuture delivering portion maintaining a suture and configured to drivean end of the suture through the septal tissue proximate the septaldefect. The repair device also includes a suture receiving portionconfigured to capture the end of the suture from the suture deliveringportion.

BRIEF DESCRIPTION OF THE DRAWINGS

The accompanying drawings are included to provide further understandingof the present disclosure and are incorporated in and constitute a partof this Specification. The drawings illustrate some of the embodimentsof the present disclosure and, together with the description, helpexplain the principles of the disclosure. Other embodiments of thepresent disclosure and many of the intended advantages of the presentdisclosure will be readily appreciated with reference to the DetailedDescription when considered in connection with the accompanyingdrawings.

In the drawings, like reference numerals designate like parts throughoutthe figures, wherein:

FIG. 1A shows a plan view of an embodiment repair device in accordancewith the present disclosure.

FIG. 1B shows a cross-sectional view along line 1B-1B of FIG. 1A.

FIG. 1C illustrates an enlarged view of the area designated 1C in FIG.1B.

FIG. 2A is a cross-sectional view of the repair device of FIG. 1Asimilar to that of FIG. 1B, with first and second units in an expandedstate.

FIG. 2B illustrates an end view of the repair device of FIG. 1A, withthe first and second units in an expanded state.

FIGS. 3 to 12B illustrate a method of repairing a septal defect inaccordance with the present disclosure.

FIG. 13A is a cross-sectional view along a central axis Y of anotherembodiment first unit of a repair device in accordance with the presentdisclosure.

FIG. 13B is an end view of the alternative embodiment of FIG. 13A.

FIG. 14 is a cross-sectional view along a central axis Y of yet anotherembodiment repair device in accordance with the present disclosure.

DETAILED DESCRIPTION

In the following Detailed Description, reference is made to theaccompanying drawings, which form a part hereof, and in which is shownby way of illustration specific embodiments in which the disclosure maybe practiced. In this regard, directional terminology, such as “top,”“bottom,” “front,” “back,” “leading,” “trailing,” etc., is used withreference to the orientation of the figure(s) being described. Becausecomponents of embodiments of the present disclosure can be positioned ina number of different orientations, the directional terminology is usedfor purposes of illustration and is in no way limiting. It is to beunderstood that other embodiments may be utilized and structural orlogical changes may be made without departing from the scope of thepresent disclosure. The following detailed description, therefore, isnot to be taken in a limiting sense, and the scope of the presentdisclosure is defined by the appended claims.

One embodiment of a catheter delivered septal defect repair device 20 inaccordance with the present disclosure is provided in FIGS. 1A and 1B.The repair device 20 is configured for delivery into a body of a patient(not shown) via a catheter introduced into a bodily lumen of thepatient, such bodily lumen including veins and/or arteries of thepatient (not shown). The repair device 20 defines a central axis X andcomprises a first unit 22. The first unit 22 includes a body 24 definingan inner lumen 26 and an expansion assembly 28 defining a suturereceiving portion 29 of the repair device 20. In one embodiment, therepair device 20 further comprises a second unit 30. The second unit 30includes a body 32 defining an inner lumen 34, an expansion assembly 35,and a suture delivering portion 36. In general terms, the repair device20 can be configured to incorporate a “nested” design in order tofacilitate its introduction into a body of a patient (not shown) viacatheter insertion. As such, in one embodiment, the first unit 22 isconfigured for insertion into a catheter and to also accept at least aportion of the second unit 30 within the inner lumen 26 of the firstunit 22. With this configuration, for example, both the first unit 22and the second unit 30 can be concurrently inserted into the body of thepatient via subcutaneous methods. However, the operative efficacy of therepair device 20 will be made clearer with reference to the text thatfollows.

In one embodiment, the first unit body 24 is tubular defining an outertransverse perimeter. They body 24 can be formed of a metallicmaterials, such as Nitinol®, plastics, or materials similar to thoseknown for use in constructing catheters. The body 24 preferably definesa generally rectangular outer transverse perimeter in cross-section. Assuch, the body 24 preferably defines four faces 37 (FIG. 2B). However,the body 24 can also define an outer transverse perimeter having othercross-sectional shapes. In one embodiment, the body 24 defines a maximumtransverse diameter compatible with insertion into a catheter (notshown). The body 24 also defines a generally rectangular transverseperimeter of the inner lumen 26.

The first unit body 24 extends from a proximal end 40 through a lengthto a distal end 38. The inner lumen 26 also extends from the proximalend 40 to the distal end 38. Furthermore, and as will be described ingreater detail below, the first unit 22 is configured such that thefirst unit 22 can be manipulated from outside the body of the patient(not shown) to repair a septal defect (not shown). As such, in oneembodiment, the body 26 defines a length such that the proximal end 40can be manipulated from outside the body of the patient while the distalend 38 is located proximate the septal defect. However, it should beunderstood that the first unit 22 can alternatively incorporate wires orother fixtures extending from the proximal end 40 to allow externalmaneuvering of the first unit 22 while the distal end 38 of the firstunit body 26 is located inside the patient.

In one embodiment, the first unit 22 includes the expansion assembly 28such that the first unit 22 is capable of being transitioned between anexpanded state and a collapsed state. In one embodiment, the expansionassembly 28 includes a plurality of nests 42 formed in the body 24 and aplurality of projections 44, each of the plurality of projections 44maintained by a corresponding one of the plurality of nests 42. As willbe described below, each of the plurality of projections 44 ismaintained within a respective one of the plurality of nests 42 with apin 45 and an actuation wire 67. Although the expansion assembly 28includes the above-described features, it should be understood that theexpansion assembly 28 can also include, springs, balloons, or otherexpandable structures without departing from the scope of the presentdisclosure.

In one embodiment, each one of the plurality of nests 42 is generallyrectangular in shape and is formed lengthwise in the body 24. A firstone of the plurality of nests 42 defines a proximal end 46, a lengthwisemidpoint 48, and a distal end 50. While the first one of the pluralityof nests 42 is described in greater detail herein, it is to beunderstood that a remainder of the plurality of nests 42 can incorporatesimilar features to those described in association with the first one ofthe plurality of nests 42. In one embodiment, each one of the pluralityof nests 42 is preferably disposed radially about the body 24. As such,one embodiment includes four nests 42, each of the four nests 42 formedin a respective one of the faces 37 of the body 24. As shown, each oneof the plurality of nests 42 is formed through a thickness of the body24. However, it is to be understood that in other embodiments, each oneof the plurality of nests 42 can be formed partially through thethickness of the body 24.

Each of the plurality of nests 42 includes a first pin track 52 (shownwith dotted lines in FIG. 1A and shown partially covered in FIG. 1B)formed in the thickness of the body 24 and extending along a nest firstside 54 from the lengthwise midpoint 48 to the distal end 50. Acorresponding second pin track 56 (shown with dotted lines in FIG. 1A)is also formed in the thickness of the body 24, extending along anopposing nest second side 58 from the lengthwise midpoint 48 to thedistal end 50. In other words, in one embodiment, each of the pluralityof nests 42 includes an opposing pair of pin tracks 52,56 extendingalong opposing nest sides 54,58. As will be described in greater detailbelow, the two pin tracks 52,56 are configured to slidably maintain thepin 45. The two pin tracks 52,56 can also be configured to rotatablymaintain the pin 45.

In one embodiment, each of the plurality of projections 44 defines aproximal end 62, a lengthwise midpoint 64, and a distal end 66. In oneembodiment, each of the plurality of projections 44 is configured suchthat an actuation wire 67 can be affixed to the proximal end 62.

The plurality of projections 44 can be generally similar in size to thecorresponding nests 42. As such, in one embodiment, each of theplurality of projections 44 is a generally rectangular and flat petal.However, each of the plurality of projections 44 is not as wide or aslong as the nest 42 in which it is maintained. In this manner, theplurality of projections 44 can be maintained in the corresponding oneof the nests 42 without interfering with either of the opposing sides54,58 or proximal and distal ends 46,50. Furthermore, each of theplurality of projections 44 is configured to be maintained within thecorresponding nest 42 without protruding from the outer transverseperimeter of the body 24 when the first unit 22 is in the collapsedstate.

As shown in FIGS. 1A and 1B, each of the plurality of projections 44forms a pin slot 68 configured to accept the pin 45. In one embodiment,the pin slot 68 originates at a proximal end 69 proximate the proximalend 62 of the projection 44 and extends proximate to the lengthwisemidpoint 64. As shown by the dotted lines in FIG. 1B, the pin slot 68extends widthwise entirely from a first side 70 to an opposing secondside 72 through a thickness of the projection 44. In this manner, thepin 45 can be slidably retained within the pin slot 62 while remainingpartially exposed from the opposing sides 70,72 of the projection 44.

In one embodiment, the first unit 22 defines, or includes, the suturereceiving portion 29 of the repair device 20. The suture receivingportion 29 can be generally described as a suture needle retainingstructure. As shown in FIGS. 1A and 1B, each of the plurality ofprojections 44 can define at least part of the suture receiving portion29. In one embodiment, the suture receiving portion 29 includes aconical receptacle that is generally complementary in shape to a sutureneedle with a porous material at a base of the conical receptacle (notshown). Additionally, it should be understood that other materials thatcan promote frictional engagement of a suture and/or suture material(not shown) could also be employed. In another embodiment, and as shownin FIGS. 1A and 1B, the suture receiving portion 29 is defined by atleast a portion of the plurality of projections 44 being formed of amesh material suitable for capturing a suture. In an exemplaryembodiment, the plurality of projections 44 are formed of Nitinol®wire-mesh material. However, alternative suture receiving portions 29can be incorporated by the first unit 22 and defined by the plurality ofprojections 44. For example, the suture receiving portion 29 can includeforming at least a portion of the plurality of projections 44 of arelatively soft material. In other embodiments, the suture receivingportion 29 can also include detents, magnets, adhesives, lockingmechanisms or other features suited to suture needle capture. It will beunderstood with reference to the text that follows that the second unit30 can also define, or include, a suture receiving portion of the repairdevice 20.

In one embodiment, the pin 45 defines a pin central portion 70, a pinfirst end 72, and an opposing pin second end 74. The pin 45 can be asolid rod formed of a material such as Nitinol®. As shown in FIG. 1B,the pin 45 defines a generally circular transverse cross-section. Inalternative embodiments, the pin 45 can also define a cam shape intransverse cross-section.

In one embodiment, the actuation wire 67 is adapted to be affixed to theproximal end 46 of the corresponding projection 44. Furthermore, theactuation wire 67 preferably defines a length such that a proximal end76 of the actuation wire 67 can be manipulated from a point outside ofthe body of the patient (not shown) while a distal end 78 of theactuation wire 67 is affixed to the corresponding projection 44. Theactuation wire 67 can be formed of a variety of materials, but in oneembodiment is formed of Nitinol® wire. As will become more evidentbelow, the actuation wire 67 is configured such that an operator (notshown) manipulating the proximal end 76 of the actuation wire 67 canpush and/or pull the wire in order to transition the first unit 22between the expanded and the collapsed states.

The repair device 20 is shown in FIGS. 1A and 1B with the first unit 22in a collapsed state. The plurality of projections 44 and the pluralityof nests 42 are preferably assembled together to define the collapsedstate shown in FIGS. 1A and 1B as follows. The plurality of projections44 are maintained within corresponding ones of the plurality of nests 42such that the plurality of projections 44 do not protrude, or extendoutwardly from, the corresponding nest 42. In other words, the pluralityof projections 44 generally lie “in plane” with the corresponding nests42 and a surrounding portion of the body 24.

As alluded to above, the pin 45 acts to help maintain the projection 44in the corresponding nest 42, as the central portion 70 of the pin 45 isslidably maintained in the pin slot 68. Further, the pin first end 72 isslidably maintained in the first pin track 52 and the pin second end 74is slidably maintained in the second pin track 56. With thisarrangement, the pin 45 can be slid within both the pin slot 68 and theopposing pin tracks 52,56. Further, the pin slot 68, the opposing pintracks 52,56, or both, can be configured to allow the pin 45 to rotate.As will be described below, such a configuration allows the projection44 to be moved distally within the corresponding nest 42 in which itresides, while also allowing the distal end 66 of the projection 44 torotate outward away from the body 24 to the position shown in FIGS. 2Aand 2B.

Additionally, it is to be understood that tension on the actuation wire67 aids in maintaining the corresponding projection 44 “in plane” asshown. In one embodiment, the actuation wire 67 extends through achannel 80 formed through the thickness of the body 24. In particular,the actuation wire 67 extends proximally beyond the body proximal end40. However, the actuation wire 67 can alternatively take an externalpath to the body 36 to extend beyond the body proximal end 40. Further,the actuation wire 67 can also extend over an internal path, e.g.,within the inner lumen 26, to extend beyond the body proximal end 40. Inone embodiment, the actuation wire 67 extends a sufficient length suchthat an operator (not shown) is capable of manipulating the actuationwire proximal end 76 from outside the body of the patient (not shown).

With reference from FIGS. 1A and 1B to FIGS. 2A and 2B, a manner oftransitioning the first unit 22 from the collapsed state (FIGS. 1A and1B) to the expanded state (FIGS. 2A and 2B) follows. In particular, theactuation wire 67 is moved forward, or distally, resulting in thecorresponding projection 44 sliding distally over the pin 45 associatedtherewith. In one embodiment, the distal end 66 of the projection 44 isconfigured such that it is guided by a distal end 50 of thecorresponding nest 42 outward from the central longitudinal axis X. Inthis manner, the projection 44 will also rotate about the pin 45. In oneembodiment, the actuation wire 67 is affixed to the proximal end 62 ofthe corresponding projection 44. As shown in FIG. 1B, the actuation wire67 can be affixed to the proximal end 62 at an offset in order tofacilitate the outward extension, or deflection of the projection distalend 66. In other words, distal movement of the actuation wire 67 can bepartially directed toward the central longitudinal axis X by the offsetin order to push the proximal end 62 of the corresponding projection 44inward towards the central longitudinal axis X. As shown, the distal end66 of the projection 44 then deflects, or projects, outward from acentral longitudinal axis X of the first unit body 24.

As the projection 44 slides distally and rotates outwardly, the pin 45eventually reaches the proximal end 69 of the pin slot 68. In oneembodiment, the projection 44 extends at a perpendicular angle to thecentral longitudinal axis X when the pin 45 has reached the pin slotproximal end 69. The continued distal actuation, or pushing, of theactuation wire 67 can then result in further distal movement of theprojection 44. In particular, the pin 45 will slide distally within thetwo opposing pin tracks 52,54. Additionally, in one embodiment, the pin45 will slide in this manner after the projection 44 has been extendedperpendicularly to the central longitudinal axis X.

Additional means of accomplishing this perpendicularly extended anddistal actuation will be recognized by those of ordinary skill in theart. For example, in one embodiment, this type of actuation is partiallyaccomplished by the pin 45 defining a cam capable of interacting withthe pin tracks 52,54, or alternatively the pin slot 68. However, camstructures are simply one means of causing the plurality of projections44 to arrest rotation at a perpendicular position relative to thecentral longitudinal axis X. For example, those having ordinary skill inthe art will recognize that stops, additional linkages, or otherfeatures can also be implemented to accomplish such movement.

The plurality of projections 44 will preferably take the position shownin FIGS. 2A and 2B once the corresponding pins 45, and consequently, theplurality of projections 44, have been slid to the distal end 50 of thecorresponding nests 42. In this position, a proximal portion of theplurality of projections 44 will preferably abut against a portion ofthe first unit body 24 defining the nest distal end 50. Distalactuation, or pushing, of the corresponding actuation wires 67 willpreferably act to support the projections 44 in this perpendicularlyextended position, while also maintaining the projections 44 at thedistal end 50 of the respective nests 42.

It should also be recognized that the first unit 22 can be collapsed, ortransitioned from the expanded to the collapsed state shown in FIGS. 1Aand 1B. In particular, transitioning the first unit 22 from the expandedstate to the collapsed state includes proximal actuation, or pulling, ofthe actuation wires 67 to effectuate a reverse series of events to thosedescribed in association with expansion of the first unit 22. In otherwords, expanding the first unit 22 includes pushing on the actuationwires 67, while collapsing the first unit 22 includes pulling on theactuation wires 67. However, those of ordinary skill in the art willrecognize that alternative means of either expanding, or collapsing thefirst unit 22, and in particular, actuation of the plurality ofprojections 44, can be employed. For instance, in alternativeembodiments, spring mechanisms can be included in the first unit 22 inorder to facilitate expanding or collapsing the first unit 22.

Returning to FIGS. 1A and 1B, and turning now to the second unit 30, thesecond unit body 32 is tubular defining an outer transverse perimeter inone embodiment. Generally, the second unit body 32 can be formed withsimilar materials to those forming the first unit body 24. In oneembodiment, the second unit body 32 defines a generally rectangularouter transverse perimeter in cross-section having a shape factorsimilar to that of the outer transverse perimeter of the first unit body24. Additionally, the second unit body 32 defines a maximum outertransverse diameter such that the second unit body 32 can be disposedwithin the inner lumen 26 defined by the first unit body 24. With theembodiment having a rectangular cross-section, the second unit body 32defines four faces 82 corresponding to the rectangular outer transverseperimeter. However, the body 32 can define other cross-sectional shapeswith the outer transverse perimeter. In one embodiment, the body 32 alsodefines a generally rectangular transverse perimeter of the inner lumen34. The second unit body 32 extends from a proximal end 84 through alength to a distal end 86. Further, the inner lumen 34 extends from theproximal end 84 to the distal end 86.

As will be described in greater detail below, the second unit 30 is alsoconfigured to be manipulated from outside the body of the patient torepair the septal defect in the body of the patient (not shown). Assuch, in one embodiment, the body 32 defines a length such that theproximal end 84 can be manipulated from outside the patient while thedistal end 86 is located proximate the septal defect. However, as withthe first unit 22, it should be noted that the second unit 30 couldalternatively incorporate additional wires or other fixtures extendingfrom the body 32 which allow external maneuvering of the second unit 30while the distal end 86 of the second unit body 32 is located inside thepatient.

In one embodiment, the second unit 30 includes the expansion assembly 35such that the second unit 30 is also capable of transitioning between anexpanded state and a collapsed state. In one embodiment, the expansionassembly 35 includes a plurality of pockets 88 formed in the second unitbody 32 and a plurality of guide bodies 90, each one of the plurality ofguide bodies 90 maintained by a corresponding one of the plurality ofpockets 88. In one embodiment, each of the plurality of guide bodies 90is maintained in a corresponding pocket 88 with a pin 92 and actuatedwith an actuation wire 94. Although embodiment expansion assemblies havebeen described as including the structures mentioned above, it should beunderstood that the expansion assembly 28 could include alternativestructures such as balloons, springs, or other expandable structureswithout departing from the scope of the present disclosure.

While one of the plurality of pockets 88 is described below in greaterdetail, it is to be understood that all of the pockets 88 canincorporate similar features. As shown in FIG. 1A, the pocket 88 isgenerally rectangular in shape and is formed lengthwise in the secondunit body 32. The pocket 88 defines a proximal end 96, a lengthwisemidpoint 98, and a distal end 100. Similarly to the first unit 22, theplurality of pockets 88 are disposed radially about the second unit body32. In particular, one embodiment includes four pockets 88, each formedin a respective one of the faces 82 of the body 32. As shown, each ofthe pockets 88 is formed through a thickness of the body 32. However, aswith the first unit 22, it is to be understood that in alternativeembodiments, the pockets 88 can be formed partially through thethickness of the body 32.

As shown in dotted lines in FIG. 1A, the pocket 88 includes a firstfemale pin mount 102 formed in the thickness of the body 32. Inparticular, the first female pin mount 102 is formed at the lengthwisemidpoint 98 in a first side 104 of the pocket 88. A corresponding secondfemale pin mount 106 is formed in an opposing second side 108. Inparticular, the second female pin mount 106 is formed in the thicknessof the body 32 at the lengthwise midpoint 98 of the pocket 88. As willbe described in greater detail below, the pin 92 is rotatably maintainedwithin the two female pin mounts 102,106. In another embodiment, thepockets 88 can incorporate structures similar to those described inassociation with the first unit 22, including opposing pin tracks formaintaining the pin 92.

While one of the plurality of guide bodies 90 is described in greaterdetail below, it is to be understood that each of the plurality of guidebodies 90 can incorporate similar features. With that in mind, the guidebody 90 defines a proximal end 110, a lengthwise midpoint 112, and adistal end 114. Additionally, guide body 90 can define a similar shapefactor to the corresponding pocket 88. However, it is to be understoodthat the guide body 90 can include tapers or rounds, such as the tapertoward the distal end 114 as shown in FIG. 1A. In one embodiment, theguide body 90 is a generally rectangular and flat petal. In oneembodiment, the guide body 90 is not as wide or as long as thecorresponding pocket 88. In particular, the guide body 90 is configuredfor reception within the corresponding pocket 88 without interferingwith either of the opposing sides 104,108 or the proximal and distalends 96,100 of the pocket 88.

In one embodiment, the guide bodies 90 are configured to be maintained“in plane” within the respective pocket 88, without protruding from theouter transverse perimeter of the body 32 when the second unit 30 is inthe collapsed state. Furthermore, when expanded, the guide bodies 90 areconfigured to extend from the central axis X less than the plurality ofprojections 44 of the first unit 22 in the expanded state. As will beunderstood with reference to the description below, this relative sizingcan facilitate suture needle capture in the suture receiving portion 29of the first unit 22. Along these lines, in one embodiment, the guidebodies 90 are formed of a solid material that can be resistant to sutureneedle penetration. In another embodiment, at least a portion of theguide bodies 90 defines the suture receiving portion 29 of the repairdevice 20.

As shown in FIGS. 1A and 1B, the guide body 90 forms a pin slot 116configured to accept the pin 92. In one embodiment, the pin slot 116originates at a proximal end 118 proximate the proximal end 110 of theguide body 90 and extends within a thickness of the guide body 90 to aslot distal end 120 proximate the lengthwise midpoint 112. As shown inFIG. 1B, the pin slot proximal end 118 begins distal to the proximal end114 such that the pin 92 can be maintained within the thickness of thepin slot 116 as it slides between the proximal and distal ends 118,120of the pin slot 116.

In one embodiment, the pin 92 is a solid rod formed of a material suchas Nitinol®. In a related embodiment, the pin 92 defines a generallycircular cross-section and defines a pin central portion 122, a pinfirst end 124, and a pin second end 126. In alternative embodiments, thepin 92 defines a cam shape in transverse cross-section.

In one embodiment, the actuation wire 94 is configured for fixation tothe proximal end 110 of the corresponding guide body 90. The actuationwire 94 defines a length such that an actuation wire proximal end 128can be manipulated from a point outside of the body of the patient (notshown) while an actuation wire distal end 130 is affixed to thecorresponding guide body 90. The actuation wire 94 can be formed of avariety of materials, but in one embodiment, is formed of Nitinol® wire.

The suture delivering portion 36 can be described in greater detail withreference to FIGS. 1A, 1B, and 1C. In one embodiment, the suturedelivering portion 36 includes a plurality of push member assemblies132. In an exemplary embodiment, the number of push member assemblies132 corresponds to the number of guide bodies 90 of the expansionassembly 36. With reference to FIG. 1C, each of the push the memberassemblies 132 includes a needle catheter 134, a push member 136disposed within the needle catheter 134, a needle 138 removably affixedto the push member 136, and a suture 140 affixed to the needle 138.While one of the push member assemblies 132 is described in greaterdetail below, it is to be understood that each of the plurality of pushmember assemblies 132 can incorporate similar features.

With reference to FIG. 1A, in one embodiment, the needle catheter 134defines a proximal end 142 and extends a length to define a distal end144. The needle catheter 134 can be of a type similar to those generallyknown in the art. The length of the needle catheter 134 extendssufficiently such that the proximal end 142 of the needle catheter 134can be manipulated from outside the body of a patient (not shown) whilethe catheter distal end 142 is affixed to the distal end 114 of thefirst one of the plurality of projections 90. Manners of affixing thedistal end 142 to the distal end 114 include such techniques as sonic orlaser welding, for example. In one embodiment, the outer diameter of theneedle catheter 134 is such that a plurality of needle cathetersincluded in the plurality of push member assemblies 132 and similar tothe needle catheter 134, can be disposed within the inner lumen 34 ofthe second unit body 32. The inner diameter of the needle catheter 134is preferably such that the push member 136 can be disposed within theneedle catheter 134.

In one embodiment, the push member 136 defines a proximal end 146 andextends a length to a distal end 148. As mentioned above, the pushmember 136 is disposed within the needle catheter 134. As described ingreater detail below, the length of the push member 136 preferablyextends sufficiently such that a proximal end 146 of the push member 136extends from the catheter proximal end 142 and can be manipulated fromoutside of the patient (not shown), while the distal end 148 of the pushmember 136 extends from the catheter distal end 144. The push member 136is made of a material such as Nitinol® wire, or plastic, for example. Inparticular, the push member 136 is preferably configured such that anoperator (not shown) can impart a push force on the push member proximalend 146 with a resultant push force being translated to the push memberdistal end 148.

With reference again to FIG. 1C, in one embodiment, the needle 138includes a base 150 configured to be removably affixed to the pushmember distal end 148. This relationship can be accomplished via meansgenerally known in the art, including interference fits, semi-permanentglues, operatively breakable welds, magnets, actuated clips, operativelybreakable lashes, and others. Further, the needle 138 is configured foraffixment to the suture 140. In one embodiment, the needle 138 alsoincludes a barb 152. In particular, the barb 152 can be configured toaid in capturing the needle 138 with the suture receiving portion 29 ofthe first unit 22.

In one embodiment, the suture 140 extends continuously from a first end154 to a second end 156 (FIG. 2A). As described above, the first end 154is preferably adapted to be affixed to the needle 138. In oneembodiment, the second end 156 is affixed to a needle 157 (shown indotted lines in FIG. 2A) of another one of the plurality of push memberassemblies 132.

In one embodiment, the suture delivering portion 36 defines anon-extended state, including the needle 138 residing within the needlecatheter 134 proximate the needle catheter distal end 144. The pushmember 136 can then be moved distally from outside the body of thepatient (not shown) to transition to the suture delivering portion 36 toan extended state such that the needle 138 extends from the needlecatheter distal end 144 sufficiently to drive the needle 138 through theseptum as desired (not shown).

The repair device 20 is shown in FIGS. 1A and 1B with the second unit 30in the collapsed state. The plurality of guide bodies 90 and theplurality of pockets 88 are preferably assembled together to define thecollapsed state as follows. Each of the plurality of guide bodies 90 ismaintained within a corresponding one of the plurality of pockets 88such that the plurality of guide bodies 90 do not protrude, or extendoutwardly from the corresponding pockets 88. In other words, theplurality of guide bodies 90 generally lie “in plane” with thecorresponding pocket 88 and a surrounding portion of the second unitbody 32.

As alluded to above, the pin 92 acts to help maintain the correspondingguide body 90 within the respective pocket 88. In particular, the pincentral portion 122 is rotatably and slidably maintained in the pin slot116 while the pin ends 124,126 are maintained in the female pin mounts102,106. With this arrangement, the pin 92 can be slid within the pinslot 116 and rotated about the pin 92. Further, the female pin mounts102,106 can also be configured to allow the pin ends 124,126 to rotatewithin them. As will be described in greater detail below, rotation ofthe guide body 90 about the pin 92 can facilitate extension of thedistal end 114 of the guide body 90 from the corresponding pocket 88 ina manner somewhat similar to that described in association with thefirst unit 22.

In one embodiment, the actuation wires 94 extend through a correspondingchannel 166 formed through the thickness of the second unit body 32. Inparticular, each actuation wire 94 preferably extends proximally beyondthe body proximal end 84. However, each actuation wire 94 canalternatively take an external path to the body 32 to extend beyond thebody proximal end 84. Further, each actuation wire 94 can also extendover an internal path, e.g., within the inner lumen 34, to extend beyondthe body proximal end 84. In one embodiment, the actuation wire proximalend 128 extends a sufficient length such that an operator (not shown) iscapable of manipulating the actuation wire proximal end 128 from outsidethe patient (not shown). As described below, pulling or proximal forceon the actuation wire 94 can act to maintain the corresponding guidebody 90 “in plane” as shown in FIGS. 1A and 1B, while pushing or distalforce on the actuation wire 94 acts to extend the corresponding guidebody 90 “out of plane.”

As mentioned above, each of the plurality of push member assemblies 132can be affixed to the corresponding distal end 114 of a respective oneof the plurality of guide bodies 90. More specifically, the distal end44 of the needle catheter 134 is affixed to the distal end 114 such thatthe lumen of the needle catheter 134 is arranged perpendicularly to thelength of the corresponding guide body 90. In this manner, the lumen ofthe needle catheter 134 can be directed toward a septum (not shown) whenthe second unit 30 is in the expanded state. Means of affixing theneedle catheter 134 to the corresponding guide body 90 can include thosegenerally known in the art, including, but not limited to, welds, glues,magnets, lashes, clamps, and others.

With reference from FIGS. 1A and 1B to FIGS. 2A and 2B, a manner ofexpanding the second unit 30 from the collapsed state (FIGS. 1A and 1B)to the expanded state (FIGS. 2A and 2B) follows. In particular, pushing,or distal movement of the actuation wires 94 preferably results in theplurality of guide bodies 90 sliding distally on the corresponding pinslot 116 over the respective pin 92. In one embodiment, the distal end110 of the each of the plurality of guide bodies 90 is configured suchthat it is guided by the distal end 100 of the corresponding pocket 88outward from the central longitudinal axis X as it is moved distally bythe corresponding actuation wire 94. In this manner, each of theplurality of guide bodies 90 will preferably also rotate about thecorresponding pin 92 as it moves distally. In one embodiment, theactuation wires 94 are connected to the proximal end 110 of thecorresponding guide body 90 at an offset toward the central longitudinalaxis X. In the embodiment, this configuration aids in directing theproximal end 110 toward the longitudinal axis X, resulting in directionof the distal end 114 outward, away from the longitudinal axis X in asliding “see-saw” manner.

As the guide body 90 slides distally and the distal end 114 rotatesoutwardly, the pin 92 eventually reaches the proximal end 118 of the pinslot 116. Once the proximal end 118 has been reached, the guide body 90extends at a perpendicular angle to the central longitudinal axis X. Inlight of the description provided herein, means of accomplishing thisperpendicular extension via distal actuation, or pushing, will berecognized by those having ordinary skill in the art. For example, onesuch means includes incorporation of a cam structure into the pin 92configured to interact with the female pin mounts 102,106 and/or the pinslot 116. A manner of retaining the guide bodies 90 in the perpendicularposition shown includes maintaining the actuation wire 94 in a fixedposition after the corresponding guide body 90 has been extended.

Similarly to the first unit 22, it should also be recognized that thesecond unit 30 can be collapsed, or transitioned from the expanded stateto the collapsed state shown in FIGS. 1A and 1B. In particular,transitioning the second unit 30 from the expanded state to thecollapsed state can include proximal actuation, or pulling, of theactuation wires 94 to effectuate a reverse series of motions to thosedescribed in association with expansion of the second member 30. Inother words, expanding the second unit 30 includes pushing on theactuation wires 94, while collapsing the second unit 30 includes pullingon the actuation wires 94. However, those of ordinary skill in the artwill recognize that alternative means of either expanding, or collapsingthe second unit 30, and in particular, actuation of the plurality ofguide bodies 90, can be employed. For instance, in alternativeembodiments, spring mechanisms or balloons can be included in the secondunit 30 in order to facilitate expanding or the collapsing the secondunit 30.

As mentioned above, the first and second units 22,30 are configured forcatheter insertion into the body of the patient (not shown). Generally,the first unit 22 is slidably disposed about the second unit 30. Morespecifically, the first unit body 24 is slidably disposed about thesecond unit body 32, such that the second unit 30 can be extended fromthe first unit body 24 but cannot be rotated therein. In one embodiment,an operator (not shown) manipulates the first unit body proximal end 40and the second unit body proximal end 84 from outside the body of thepatient (not shown) to effectuate relative extension. With thisconfiguration, the suture delivering portion 36 of the second unit 30can be extended while remaining aligned with the suture receivingportion 29 of the first unit 22. For example, and as shown in FIGS. 1A,1B, 2A and 2B, the non-rotatable configuration allows both units 22,30to be transitioned to the expanded state with the second unit pluralityof guide bodies 90 aligned with the first unit plurality of projections44.

As such, the second unit 30 is extended from the first unit inner lumen26 prior to transitioning to the expanded state in the manner describedabove. As will be described in greater detail below, this slidable andnested configuration also allows the repair device 20 to reside on twosides of a septal defect (not shown) in order to opposingly anchor thestructures surrounding the septal defect between the two units 22, 30.

Additionally, the first unit 22 can alternatively be configured to bedisposed within the second unit 30. Indeed, it is to be understood thatin embodiments of the present disclosure, the features described inassociation with the first and second units are interchangeable. Forexample, the first unit 22 can include the suture delivering portion 36while the second unit 30 includes the suture receiving portion 29.

With that in mind, and with reference to FIGS. 3-12B, a system andmethod of repairing a congenitally defective heart 200 can be described.For those not familiar with the nomenclature commonly associated withcardiac structures, the designation “left” or “right” corresponds to the“left” and “right” of the patient (not shown) and should be interpretedaccordingly. The heart 200 is shown from a front of the patient (notshown) and generally includes a right atrium 202, a left atrium 204, aright ventricle 206, and a left ventricle 208. An inferior vena cava 210and a superior vena cava 212 also lead into the right atrium 202. Aseptum divides the heart 200 into a right half and a left half. Morespecifically, the septum includes an atrial septum 214 and a ventricularseptum 216. The atrial septum 214 separates the right and left atria202,204 while the ventricular septum 216 separates the right and leftventricles 206, 208.

The atrial septum 214 is formed by septal tissue and includes a septumprimum 218 and a septum secundum 220. Prior to childbirth the septumprimum 218 and the septum secundum 220 define a passageway for bloodbetween the right and left atria 202,204 Following childbirth, thepassageway will close in a healthy heart (not shown). As shown, theheart 200 includes a septal defect 222 in the form of such a passageway,a patent foramen ovale. In one embodiment, the patent foramen ovaleoccurs due to improper formation of the septum primum 218. In otherembodiments, the patent foramen ovale occurs due to improper formationof the septum secundum 220, or both the septum primum 218 and the septumsecundum 220.

Furthermore, while embodiment methods of repairing a congenital heartdefect will be described in association with the septal defect 222including the patent foramen ovale, it is to be understood that theprinciples and embodiments described herein can be applied to othertypes of congenital heart defects, including, for example, ventricularseptal defects.

In one embodiment, a guide wire 225 is introduced into the body of thepatient (not shown) via a sheath in the femoral artery (not shown). Theguide wire 225 is introduced into the heart 200 in a manner known in theart. In one embodiment, the guide wire 225 is a J-Tip wire. A guidecatheter 226 is then threaded over the guide wire 225 and into the heart200. Generally, the guide catheter 226 will be introduced into one ormore bodily lumens and delivered to the heart 200. In one embodiment, adistal portion 228 of the guide catheter 226 is guided from one bodilylumen the femoral artery to the heart 200 via the inferior vena cava 210and into a right atrium 202. In an alternative embodiment, the heart 200can be entered from a left atrial or left ventricular side. However,such an approach is known to increase the risk of forming blood clots.The guide catheter 226 so disposed includes a proximal portion (notshown) of the guide catheter 226 remaining exposed outside of the bodyof the patient. Further, the guide catheter 226 is preferably configuredsuch that the distal portion 228 is capable of being selectively angledby an operator (not shown) from outside of a body of a patient (notshown) toward the septal defect 222.

With reference to FIG. 4, one embodiment method of guiding the repairdevice 20 into the left atrium 204 via the guide catheter 226 includespiercing, or puncturing, the septum 214 with a transseptal needle 234.In one embodiment, the repair device 20 (hidden in FIG. 4) is guidedinto the left atrium 204 over the guide wire 225 (FIG. 3) through theguide catheter 226. More specifically, once the guide catheter 226 andguide wire 225 have been disposed within the right atrium 202, therepair device 20 is preferably threaded over the guide wire 225, throughthe guide catheter 230, and into the right atrium 202. As discussedabove, the second unit 30 is preferably slidably disposed within thefirst unit 22. In one embodiment, the guidewire 225 is then removed andreplaced with the transseptal needle 234. As described above, the guidecatheter 226 is angled toward the septal defect 222 in order to directthe repair device 20 and the transseptal needle 245 to the septal defect222. In another embodiment, the repair device 20 is configured such thatthe repair device 20 can be selectively angled toward the septal defect222 to guide the transseptal needle 245 proximate the septal defect 222.

In one embodiment including an inter cardiac echo catheter, the repairdevice 20 is guided under inter cardiac echo to a desired positionproximate the septal defect 222. In one exemplary embodiment, thedesired position is proximate the septum primum 218. Once properlypositioned, the transseptal needle 234 is used to puncture the atrialseptum 214. In one embodiment, the septal tissue defining the septumprimum 218 and the septum secundum 220 is punctured. Once the septaltissue defining the atrial septum 214 has been punctured, thetransseptal needle 234 extends between the right atrium 202 and the leftatrium 204. The repair unit 20 is extended from the guide catheter 226and over the transseptal needle 234 as shown in FIG. 5. The transseptalneedle 234 is removed from the repair device 20 and out of the body ofthe patient (not shown).

With reference from FIG. 5 to FIG. 6, the second unit 30 is preferablysufficiently advanced into the left atrium 204 such that the second unit30 can transition to the expanded state. Once the second unit 30 hasbeen sufficiently advanced, the transseptal needle 234 (not shown) canbe removed from the repair device 20 and taken completely out of thepatient (not shown).

Other methods of guiding the repair device 20 from the right atrium 202to the left atrium 204 can also be employed. Another embodiment methodof delivering the repair device 20 from the right atrium 202 to the leftatrium 204 includes removing the guide wire 225 from the guide catheter226 and inserting a transseptal needle 234 into the guide catheter 226prior to inserting the repair device 20 into the guide catheter 226. Inparticular, the transseptal needle 234 is guided to the atrial septum214 proximate the septal defect 222. The transseptal needle 234 is thenused to puncture the atrial septum 214, and in one embodiment, theseptum primum 218 and septum secundum 220. The guide catheter 226 canthen be guided over the transseptal needle 234 into the left atrium 204.The transseptal needle 234 is removed from the guide catheter 226 andreplaced with the repair device 20. The repair device 20 can then bedelivered into the left atrium 204 via the guide catheter 226. Inanother embodiment method of guiding the repair device 20 into the rightatrium 202, the atrial septum 214 is punctured with a suitablyconfigured tip of the guide catheter 226, or alternatively, the repairdevice 20, to deliver the repair device 20 to the left atrium 204. Inyet another embodiment, the guide catheter 226 is guided through theseptal defect 222 itself to the left atrium 204 without puncturing theatrial septum 214. In another embodiment, the repair device 20 is guidedthrough the septal defect 222 between the atria 202,204 (i.e., theseptum 214 is not initially punctured).

With reference to FIG. 7, in one embodiment method, when the second unit30 is appropriate disposed in the left atrium 204, it is then expandedto the expanded state. The first unit 22 is also sufficiently extendedfrom the guide catheter 226 and transitioned to the expanded state. Thefirst unit 22 and the second unit 30 are then opposingly contacted witha first side 236 and a second side 238 the septum 214. In particular,the plurality of guide bodies 90 is pulled against the second side 238of the septum 214 while the plurality of projections 44 is pushedagainst the first side 236 of the septum 214. In one embodiment, thesecond unit 30, and in particular the body proximal end 84 (not shown)is pulled back, or moved proximally, in order to make contact with theatrial septum 214 while the first unit body proximal end 40 (not shown)is pushed from outside the patient (not shown). In one embodiment, andas shown in FIG. 7, the plurality of guide bodies 90 is abutted againstthe septum secundum 220 and the plurality of projections 44 arecontacted with the septum primum 218. Thus, the two units 22,30 areopposingly contacted with the septum 214. With this opposing contact,the first unit 22 and the second unit 30 press portions of the atrialseptum 214 proximate the septal defect 222 to press or perhaps anchor orlock the atrial septum 214 in place between the two units 22,30 of therepair device 20.

As mentioned above, in one embodiment, the second unit 30 is preventedfrom rotating within the first unit 20. Along these lines, the generallyrectangular cross-sections of both the first and second units 22,30 canact to prevent relative rotation of the two units 22, 30. With thisconfiguration, the plurality of projections 44 of the first unit 22 inthe plurality of guide bodies 90 of the second unit 30 are maintained inan aligned position. Particularly, each one of the plurality ofprojections 44 residing on one side of the septum 214 is aligned to acorresponding one of the plurality of guide bodies 90 residing on theopposite side of the septum 214. In one embodiment, the alignment of theplurality of guide bodies 90 with the plurality of projections 44results in each one of the plurality of push wire assemblies 132, and inparticular, the needle catheter distal end 144 being aligned with thesuture receiving portion 29 defined, or otherwise included, by each oneof the plurality of projections 44.

With reference to FIG. 8, the suture delivering portion 36 is then usedto drive the suture 140 through the atrial septum 214 at a firstlocation proximate the septal defect 222. In one embodiment, the pushmember 136 is manipulated from outside of the patient (not shown) in adistal direction to extend from the needle catheter 134. In other words,each push member 136 is pushed distally such that the needle 138 affixedto the corresponding push member 136 extends from the correspondingneedle catheter 134 and is driven through the atrial septum 214, and inparticular the tissue defining the atrial septum 214, with the suturefirst end 154 in tow. In one embodiment, both the septums primum andsecundum 218,220, are fully pierced with the first end 154 of the suture140 in tow. As shown, the needles 138 are pushed through the atrialseptum 214 and into the suture receiving portion 29 of the first unit 22to be captured or retained therein. As shown in FIG. 8, the suturereceiving portion 29 includes one of the plurality of projections 44being formed of wire mesh such that when the barb 152 of the needle 138is passed into the mesh, the needle 138 is anchored therein.

With reference to FIG. 9, the push members 136 (not shown) are thenpulled, or moved, proximally from outside the patient (not shown) inorder to retract the push members 136 back into the corresponding needlecatheter 134. As mentioned above, the needle 138 is preferably removablyaffixed to the corresponding push member 136, such that pulling, orproximal movement of the push member 136 results in separation of thepush member 136 from the needle 138. With the needle 138 captured by thesuture receiving portion 29 of the first unit 22, along with the suturefirst end 154, the push member 136 is then removed from the atrialseptum 214 and back into the needle catheter 134. As shown, the secondend 156 of the suture 140 affixed to the second needle 157, is driventhrough the tissue at a second location and anchored, or captured withinthe suture receiving portion 29 of the first unit 22 in a similarmanner. As will be described below, the two ends 154,156 can then betied together once the first unit 22 is removed from the body of thepatient (not shown) with the ends 154,156 in tow. In one embodiment,needles affixed to two ends of a second suture 158 are also driventhrough the tissue of the atrial septum 214 at a third and a fourthlocation proximate the septal defect 222 and into other ones of theplurality of projections 44 in a similar manner. It should be understoodthat embodiments of the method generally include a plurality of suturesbeing driven through the atrial septum 214 such that a first end and asecond end of each of the plurality of sutures is captured by the suturereceiving portion 29.

In one embodiment, once the suture 140 and second suture 158 have beencaptured by the first unit 22, the second unit 30 is transitioned backto the collapsed state. Following transitioning, the second unit 30 isretracted from the left atrium 204 and back within the first unit 22. Inone embodiment, a hole remains where the septum 214 was punctured uponretrieval of the second unit 30 from the left atrium 204. In anotherembodiment, the natural elasticity of the septum 214 causes the hole tocontract such that it is substantially closed.

In FIG. 10, the second unit 30 (hidden) has been retracted into thefirst unit 22. The first unit 22 also transitions back to the collapsedstate once the sutures 140, 158 have been captured. In one embodiment,the first end 154 and the second end 156 of the suture 140, and thefirst and second ends of the second suture 158 are drawn toward thecentral axis X (FIG. 1A) of the repair device 20 and into the pluralityof nests 42.

With reference to FIG. 11, the first unit 22 is retracted from the rightatrium 202 and into the guide catheter 226 with the first and secondends 154,156 of the suture 140 and the first and second ends of thesecond suture 158 in tow. In this manner, an operator (not shown) canaccess the ends of the sutures 156,158 from outside of the body of thepatient (not shown). As shown in FIG. 11, the two ends 156,158 can thenbe tied into a first knot 160, such as a simple suture. In oneembodiment, a knot pusher (not shown) is used to push the first knot 160formed in the suture 140 outside of the body of the patient back throughthe guide catheter 226 and to the atrial septum 214. The excess materialof the suture 140 surrounding the first knot 160 can then be clipped. Inone embodiment, the knot pusher includes a clipping mechanism (notshown). A similar method can be used to tie a knot 162 (FIG. 12A) in thesecond suture 158. As shown, the hole punctured in the septum 214 is atleast partially closed with the knot 162 adjacent the septum 214.

With reference to FIGS. 12A and 12B, a preferred configuration of thesutures 140, 158 and their corresponding knots 160,162 can be described.In particular, FIG. 12A shows one preferred configuration from aviewpoint of the right atrium 202. Conversely, FIG. 12B shows apreferred configuration from a viewpoint of the left atrium 204. Asshown, the two sutures 140,158 act to maintain the atrial septum 214 ina closed position in order to repair the septal defect 222 (not shown).Furthermore, in one embodiment, the hole punctured in the septum is alsodrawn closed by the two sutures 140,158. In another embodiment, thesutures 140,158 can be used to repair a hole through the ventricularseptum 216 (not shown). In another alternative embodiment, a patch (notshown) of a type known in the art can be sutured to one side of theseptum 214, or two patches can be sutured to opposing sides of theseptum 214, respectively. Regardless, the patch or patches can besecured by one or both of the sutures 140 or 158 in conjunction with theabove method, or can be affixed separately.

As alluded to above, alternative embodiments also include additionalsutures and/or patches used to repair septal defects. For example, apatch (not shown) could be delivered via the repair device 20 to thearea approximate the septal defect 222 and sutured thereto utilizing anembodiment method of the present disclosure. Additionally, anotherembodiment of the present disclosure can include suturing an occlusiondevice proximate a septal defect. Furthermore, alternative sutureconfigurations, including non-crossed configurations as otherwise shownin FIGS. 12A and 12B, are also incorporated in alternative embodiments.It is also to be understood that in one exemplary embodiment wherein thefirst unit 22 includes a suture delivering portion and the second unit30 includes a suture receiving portion, the views of FIGS. 12A and 12Bcan be reversed such that FIG. 12A would show a view from the leftatrium 204.

Although specific embodiments have been illustrated and describedherein, it will be appreciated by those of ordinary skill in the artthat a variety of alternate and/or equivalent implementations may besubstituted for the specific embodiments shown and described withoutdeparting from the scope of the present disclosure. For example, FIGS.13A and 13B illustrate an alternative embodiment first unit 321 of arepair device 320 in accordance with the present disclosure. Generally,the first unit 321 comprises a body 322 and an expansion assembly 324.In particular, the expansion assembly 324 includes a mesh hood 326 andan actuation catheter 327.

The body 322 is preferably formed of materials similar to those known inthe art. In one embodiment, the body 322 is a catheter and defines agenerally circular transverse cross-section forming an inner lumen 328.The body 322 extends from a proximal end (not shown) to a distal end332. Further, the body 322 defines a length sufficient to allowmanipulation of the proximal end while the distal end 332 is proximate aseptal defect (not shown). In one embodiment, the body 322 is configuredfor insertion into the actuation catheter 327.

The actuation catheter 327 of the expansion assembly 324 can be acatheter of a type generally known in the art. Generally the actuationcatheter 327 defines an inner lumen 334, a proximal end (not shown) anda distal end 338. As described above, the inner lumen 334 is preferablyconfigured to accept the body 322. Additionally, the actuation catheter327 preferably extends a length sufficient to allow manipulation of theproximal end from outside the body of the patient (not shown) while thedistal end 338 is disposed proximate a septal defect (not shown).

As shown in FIG. 13A, the hood 326 is affixed to the body 322. The hood326 is preferably configured to expand outwardly from a centrallongitudinal axis Y of the first unit 321 when unconstrained by theactuation catheter 327. In particular, the hood 326 can be formed ofNitinol® mesh, or another metal capable of incorporating a springaction. Alternatively, the hood 326 can be formed of expandable plasticstructure. Preferably a spring action allows the hood 326 to springbetween a configuration substantially perpendicular to the centrallongitudinal axis Y (FIG. 13B) to a configuration substantially parallelto the central longitudinal axis Y (FIG. 13A). Additionally, the hood326 is also configured to define a suture receiving portion 329 of therepair device 320. In particular, a thickness of the hood 326 isconfigured to retain a first end of a suture (not shown).

As such, assembly of the body 322 and actuation catheter 327 can bedescribed as follows. The hood 326 is affixed to the distal end 332 ofthe body 322. Preferably, both the body 322 and the hood 327 affixedthereto are slidably disposed within the inner lumen 334 of theactuation catheter 327.

A method of transitioning the first unit 321 to an expanded stateincludes sliding the body 322 and the actuation catheter 327 relative toone another such that the hood 326 is exposed from the distal end 338 ofthe actuation catheter 324. The spring action of the hood 327 causes thehood 327 to transition to a configuration substantially perpendicular tothe central longitudinal axis Y (FIG. 13B). Another alternativeembodiment a repair device further comprises a second unit substantiallysimilar to the first unit 321, but configured to be slidably disposedwithin the first unit 321. In another embodiment, the second unit issubstantially similar to the second unit 30 of the repair device 20.

Another alternative embodiment repair device 420 in accordance with thepresent disclosure is shown in FIG. 14. Generally, the repair device 420includes a body 422, an expansion assembly 424, a suture receivingportion 425, and a suture delivering portion 426.

The body 422 can be formed of materials similar to those be used inassociation with catheters known in the art. The body 422 is configuredto be coaxially received within an inner lumen of a guide catheter (notshown). The body 422 also defines a central lumen 428 of the repairdevice 420.

The expansion assembly 424 can be described as similar to thosepreviously described in association with other embodiments. Generally,the expansion assembly can include a plurality of projections 430 thatcan be actuated with actuation wires 432. In the embodiment, the repairdevice 420 includes two projections 430, a first one 434 formed of asolid material and configured such that a distal end 436 of the firstone 434 can be affixed to the suture delivery portion 426. A second one438 of the plurality of projections 430 can be formed of a wire meshmaterial to define the suture receiving portion 425 of the repairdevice.

The suture delivering portion 426 of the repair device 420 can include aneedle catheter 440, a push member 442, a suture needle 444, and asuture 446. The needle catheter 440 is configured to slidably accept thepush member 442 within an inner lumen (not shown) of the needle catheter440.

The push member 442 is configured to transition to adopt a curvilinearshape upon extension from the needle catheter 440. In particular, thepush member 442 can be made of a shape memory metal, such as Nitinol®,with a naturally occurring curve resulting in the push member when it isunconstrained by the needle catheter 440.

The suture needle 444 and the suture 446 can be largely similar to thosepreviously described. As such, the suture needle 444 can be removablyaffixed to the push member 442 at a distal end 448 of the push member442. In another embodiment, the suture needle 444 is configured totransition to adopt a curvilinear shape upon extension from the needlecatheter 440. In the embodiment shown, the suture 446, and inparticular, a first end 450 of the suture 446 is affixed to the sutureneedle 444. In another embodiment, the first end 450 is removablyaffixed to the suture needle 444.

In one embodiment, the needle catheter 440 is affixed to the first one434 of the plurality of projections 430, such that when the plurality ofprojections 430 are transitioned to an expanded state and abuttedagainst a septum 452 the suture needle is positioned at a first locationL1 proximate a septal defect 410.

In a related embodiment, the repair device 420 further includes a secondunit (not shown) similar to that of the first unit 321 of the repairdevice 320. The repair device 420 can also include a second unit (notshown) similar to the first unit 22 or the second unit 30 of the repairdevice 22. With the addition of the second unit to the repair device420, the septum (not shown) can be anchored between the expansionassembly 424 and the second unit to facilitate suturing in a mannersimilar to that described above in association with other embodiments.

As such, a method of repairing a septal defect includes expanding theplurality of projections 430 to an expanded state and abutting theplurality of projections against a first side 454 of the septum 452,such that the suture needle 444 is positioned at a first locationproximate the septal defect 410. The suture needle 444, with the firstend 450 of the suture 446 affixed thereto, is extended from the needlecatheter 440 by actuating the push member 442 from a location outside ofthe patient (not shown). As the suture needle 444 is extended from theneedle catheter 440, the suture needle 444 is driven through the septaltissue at the first location from the first side 454 to a second side456 of the septum 452. As shown in FIG. 14, the push member 442 extendsin a curvilinear manner as it is extended further from the needlecatheter 440 until the suture needle 444 is positioned at a secondlocation L2 proximate the septal defect and driven through the tissue ofthe septum 452 from the second side 456 to the first side 454 and intothe suture receiving portion 425.

The suture needle 444 is received within the receiving portion 425, andupon retraction of the push member 442 back into the needle catheter440, remains captured therein with the first end 450 of the suture 446affixed thereto and also captured accordingly. In an alternativeembodiment including the first end 450 being removably affixed to thesuture needle 444, the suture needle remains affixed to the push member442 while the first end 450 of the suture 446 is captured within thecapture portion 425 upon retraction of the push member 442. Theexpansion assembly 424 can then be transitioned back to the collapsedstate and retracted from the patient with the first end 450 of thesuture 446 in tow. In this manner, an operator can thereby tie the firstend 450 of the suture 446 and a second end (not shown) of the suture 446in order to repair the septal defect 410, or alternatively suture apatch thereto, for example.

As mentioned above, alternative embodiment repair devices can alsoinclude a balloon as an expansion means for either a first unit or asecond unit of the alternative embodiment repair device. For example, inone embodiment, the repair device includes a balloon mounted on acatheter. In particular, the balloon can define a generally hourglassshape in an expanded state, such that the balloon can anchor septaltissue proximate a septal defect between two opposing hourglass portionsof the balloon. With the alternative embodiment, a suture deliveringportion similar to that described above is mounted on one hourglassportion of the balloon while a suture receiving portion is mounted onthe opposite hourglass portion of the balloon. In one embodiment, thesuture receiving portion includes a plurality of funnels defining agenerally conical shape and having a porous material at a base of eachof the funnels. The plurality of funnels is radially disposed about theone hourglass portion of the balloon with a plurality of push wireassemblies disposed about the opposite hourglass portion of the balloon.The plurality of funnels and the plurality of push wire assemblies arealigned with one another such that a plurality of needles affixed to aplurality of suture ends can be extended from each of the plurality ofpush wire assemblies into each of the plurality of funnels followingexpansion of the balloon.

As such, one embodiment method of repairing a septal defect utilizingthe alternative embodiment repair device can include the following:guiding the repair device to an area approximate a septal defect;guiding the repair device through the septum; expanding the balloon ofthe repair device to the expanded state to press the septum; actuatingthe suture delivering portion to drive a plurality of suture endsthrough the tissue defining the septum and into the suture receivingportion of the repair device; transitioning the balloon back to acollapsed state; retracting the repair device form the body with aplurality of suture ends in tow; and tying the plurality of suture ends.

Additionally, alternative sewing assemblies, such as, for example, arepeating mechanical sewing machine are also included within the scopeof the present disclosure. For example, in another alternativeembodiment, a repeating mechanical sewing machine includes a first unitacting analogously to a bottom mechanism of a sewing machine with asecond unit including a needle pusher acting analogously to a needledriving portion of a sewing machine. In one embodiment, the two unitsare configured to be rotated in concert while aligned on opposing sidesof a septal defect. As the two units are rotated, the needle pusherrepeatedly drives a needle that is carrying a portion of a suturethrough the septum and to the first unit such that the suture iscontinuously and repeatedly driven through the septum at variouslocations proximate the septal defect. In this manner, the suture canthen be “tightened up” and the septal defect sewn shut.

In light of the above, an improved manner of repairing congenitaldefects via less invasive means, including repairing those defects notamenable to the use of occlusion devices, is presented herein. Inparticular, those of ordinary skill in the art will understand the textabove and accompanying figures to present a method and apparatus capableof allowing a surgeon to suture septal tissue proximate a septal defectwith less invasive methods than those related to accessing the heartthrough the chest of a patient. This application is intended to coverany adaptations or variations of the specific embodiments discussedherein. As such, it is intended that this disclosure be limited only bythe claims and the equivalents thereof.

1. A septal defect repair system for repairing a septal defect in aseptum defined by septal tissue, the system comprising: a guide catheterdisposed within a bodily lumen of a patient; and a repair devicedisposed within the guide catheter, the repair device including: anexpansion assembly configured to press opposing sides of the septumtogether, a suture delivering portion maintaining a first suture andconfigured to drive a first end of the suture through the septal tissueproximate the septal defect, a suture receiving portion configured tocapture the first end of the suture from the suture delivering portion.2. The system of claim 1, wherein the suture receiving portion includesa plurality of radially extendable petals.
 3. The system of claim 2,wherein the petals are pivotably coupled to a first tubular body, andfurther wherein the suture delivering portion includes a plurality ofguide bodies pivotably coupled to a second tubular body, and furtherwherein the system is configured such that in an expanded state of thepetals relative to the first tubular body and of the guide bodiesrelative to the second tubular body, respective ones of the petals arelongitudinally aligned with respective ones of the guide bodies.
 4. Thesystem of claim 3, wherein the second tubular body is slidably disposedwithin the first tubular body.
 5. The system of claim 1, wherein thesuture delivering portion includes: a tubular delivery body slidablyassociated with the suture receiving portion; first and second needlecatheters slidably connected to the delivery body and terminating at adistal end; first and second needles slidably disposed within a lumen ofa respective one of the first and second needle catheters; wherein thefirst end of the first suture is connected to the first needle and anopposing second end of the first suture is connected to the secondneedle; and further wherein the suture delivering portion is configuredto be transitionable from a collapsed state to an expanded state, aradial extension of the distal ends relative to the delivery body beinggreater in the expanded state than in the collapsed state.
 6. The systemof claim 5, wherein the suture delivery portion further includes: thirdand fourth needle catheters slidably connected to the delivery body andeach terminating at a distal end; third and fourth needles slidablydisposed within a lumen of a respective one of the third and fourthneedle catheters; a second suture having a continuous length andterminating at opposing, first and second ends; wherein the first end ofthe second suture is connected to the third needle and the second end ofthe second suture is connected to the fourth needle; and further whereinthe expanded state includes the distal ends of the third and fourthneedle catheters being radially spaced from an exterior of the deliverybody.
 7. The system of claim 6, wherein the expanded state includes thedistal end of the first and second needle catheters extending inopposite directions from the delivery body, and the distal end of thethird and fourth needle catheters extending in opposite directions fromthe delivery body.
 8. The system of claim 5, wherein the suturedelivering portion further includes first and second guide bodiespivotably coupled to the delivery body, the first guide body attached tothe first needle catheter and the second guide body attached to thesecond needle catheter.
 9. The system of claim 8, wherein the system isconfigured such that transitioning between the collapsed and expandedstates includes the guide bodies pivoting relative to the delivery body.10. The system of claim 1, wherein the suture delivering portionincludes a tubular delivery body maintaining a plurality of radiallyextendable guide bodies, wherein the suture receiving portion includes atubular carrying body maintaining a plurality of radially extendableprojections, and further wherein the delivery body and the carrying bodyare rotationally affixed relative to one another.
 11. The system ofclaim 10, wherein the delivery body is slidably disposed within thecarrying body.
 12. The system of claim 1, wherein the suture receivingportion includes a wire mesh material.
 13. The system of claim 1,wherein the suture receiving portion includes a plurality of conicalreceptacles, each receptacle including a porous material at the base ofthe receptacle.
 14. The system of claim 1, wherein the suture deliveringportion includes at least one needle configured to take a curvilinearshape, the needle maintaining the end of the suture.
 15. The system ofclaim 1, wherein the suture delivering portion includes a plurality ofpush wire assemblies, each one of the plurality of push wire assembliesincluding: a needle catheter; a push member slidably disposed within theneedle catheter; and a suture needle removably affixed to an end of thepush wire; wherein the end of the suture is affixed to the suture needleand the suture receiving portion is configured to capture the end of thesuture from the suture delivering portion by capturing the sutureneedle.
 16. The system of claim 15, wherein the push member isconfigured to take a curvilinear shape upon extension from the needlecatheter.